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The side effects of immune checkpoint inhibitor therapy on the endocrine system.

Authors :
Goyal, Itivrita
Pandey, Manu Raj
Sharma, Rajeev
Chaudhuri, Ajay
Dandona, Paresh
Source :
Indian Journal of Medical Research. Oct2021, Vol. 154 Issue 4, p559-572. 14p.
Publication Year :
2021

Abstract

Immune checkpoint inhibitors (ICIs) are a relatively newer class of drugs approved for the treatment of malignancies such as melanoma, renal, bladder and lung cancer. Immune-related adverse events (IrAEs) involving the endocrine system are a common side effect of these drugs. The spectrum of endocrine adverse events varies by the drug class. Cytotoxic T-lymphocyte-associated antigen-4 inhibitors commonly cause hypophysitis/hypopituitarism, whereas the incidence of thyroid disease is higher with programmed cell death (PD)-1/ligand (PD-L) protein 1 inhibitors. The focus of this review is to describe the individual endocrinopathies with their possible mechanisms, signs and symptoms, clinical assessment and disease management. Multiple mechanisms of IrAEs have been described in literature including type II/IV hypersensitivity reactions and development of autoantibodies. Patients with preexisting autoimmune endocrine diseases can have disease exacerbation following ICI therapy rather than de novo IrAEs. Most of the endocrinopathies are relatively mild, and timely hormone replacement therapy allows continuation of ICIs. However, involvement of the pituitary-adrenal axis could be lifethreatening if not recognized. Corticosteroids are helpful when the pituitary-adrenal axis is involved. In cases of severe endocrine toxicity (grade 3/4), ICIs should be temporarily discontinued and can be restarted after adequate hormonal therapy. Endocrinologists and general internists need to be vigilant and maintain a high degree of awareness for these adverse events. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09715916
Volume :
154
Issue :
4
Database :
Academic Search Index
Journal :
Indian Journal of Medical Research
Publication Type :
Academic Journal
Accession number :
156756496
Full Text :
https://doi.org/10.4103/ijmr.IJMR_313_19